Dapagliflozin Patient Satisfaction Survey
- Conditions
- Diabetes Mellitus, Type 2
- Registration Number
- NCT02805283
- Lead Sponsor
- AstraZeneca
- Brief Summary
The purpose of this study is to evaluate the diabetes related treatment satisfaction for patients with type 2 diabetes mellitus
- Detailed Description
This is a cross-sectional, observational patient survey study. Study subjects will be adult commercial members of the large US health plan affiliated with Optum with evidence of T2D initiating dapagliflozin or a sulfonylurea medication within the 3 months prior to survey mailing.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 653
- At least one pharmacy claim for dapagliflozin or dapagliflozin/metformin ER in the most recent month of pharmacy data and no pharmacy claims for an SGLT2 medication during the 6 months prior to sample identification.
- Evidence of T2D diagnosis.
- Age ≥18 as of the drug index date.
- 6 months of continuous enrollment in a commercial health plan with both pharmacy and medical benefits during the identification period through the patient interview sample identification date.
- Self-reported T2D diagnosis during the patient interview.
- Patients with evidence of type 1 diabetes mellitus and unknown type
- Patients who are pregnant
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Condition-specific treatment satisfaction 2 weeks Condition-specific treatment satisfaction as measured by the Diabetes Treatment Satisfaction Questionnaire (DTSQ)
- Secondary Outcome Measures
Name Time Method Self-reported body weight 1 month Self-reported body weight
Hypoglycemia Fear Survey 4 weeks Fear of hypoglycemia (HFS)
Medical Outcomes Study (MOS) Short Form Health Survey SF-12 or SF-36 4 weeks MOS Short Form Health Survey SF-12 or SF-36
Morisky Medication Adherence Scale 1 month Medication adherence
Trial Locations
- Locations (1)
Reasearch Site
🇺🇸Eden Prairie, Minnesota, United States